4380-96-5

Basic information

• Product Name: 2,2'-BITHIOPHENE-5-METHYLAMINE
• Synonyms: 5-(Aminomethyl)-[2,2']-bithiophene;5(Thien-2-yl)then-2-ylamine;2,2'-bithiophen-5-ylMethanaMine;C-[2,2']BITHIOPHENYL-5-YL-METHYLAMINE;2-AMINOMETHYL-5-(THIEN-2-YL)THIOPHENE;2,2'-BITHIOPHENE-5-METHYLAMINE;5-(THIEN-2-YL)THIEN-2-YLMETHYLAMINE;RARECHEM AL BW 1310
• CAS NO: 4380-96-5
• Molecular Formula: C₉H₉NS₂
• Molecular Weight: 195.3
• Mol File: 4380-96-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 71-73°C
• Boiling Point: 128 °C
• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,2'-BITHIOPHENE-5-METHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-BITHIOPHENE-5-METHYLAMINE(4380-96-5)
• EPA Substance Registry System: 2,2'-BITHIOPHENE-5-METHYLAMINE(4380-96-5)

Safety Data

• Hazard Codes: C,T
• Statements: 34-25
• Safety Statements: 26-36/37/39-45
• RIDADR: 3259
• Hazardous Substances Data: 4380-96-5(Hazardous Substances Data)

Usage

General Description

2,2'-Bithiophene-5-methylamine is a chemical compound that belongs to the bithiophene family, which consists of fused ring structures containing two thiophene rings. It is a substituted derivative with a methylamine group attached to the 5-position of one of the thiophene rings. 2,2'-BITHIOPHENE-5-METHYLAMINE has potential applications in the field of organic electronics and materials science, particularly as a building block for the synthesis of organic semiconductors and conductive polymers. It may also have uses in the development of new materials for electronic and optoelectronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Further research and development of 2,2'-bithiophene-5-methylamine could lead to advancements in the production of more efficient and sustainable electronic technologies.

Upstream product

• 632338-98-8 [4-(thien-2-yl)-thien-2-yl]methylazide 
• 492-97-7 2,2'-Bithiophene 
• 3515-30-8 5-hydroxymethyl-2,2'-bithiophene 
• 256327-11-4 N-[2,2']bithiophenyl-5-ylmethyl-phthalamic acid 
• 3480-11-3 5-bromo(2,2'-bithiophene) 

Downstream Products

• 256327-11-4 N-[2,2']bithiophenyl-5-ylmethyl-phthalamic acid 
• 1201809-65-5 C₂₃H₂₉N₇S₂ 

Relevant articles and documents

One-pot primary aminomethylation of aryl and heteroaryl halides with sodium phthalimidomethyltrifluoroborate

A one-pot primary aminomethylation of aryl halides, triflates, mesylates, and tosylates via Suzuki-Miyaura cross-coupling reactions with sodium phthalimidomethyltrifluoroborate followed by deamidation with ethylenediamine is reported.

1,2 DIAMIDO CYCLOALKYL SODIUM CHANNEL BLOCKERS

1,2 Diamido cycloalkyl compounds that are sodium channel blockers; pharmaceutical compositions that include an effective amount of the aryl-link-aryl thiazolidin-dione and aryl-link-aryl oxazolodine-dione compounds and a pharmaceutically acceptable carrier; and a method of treatment of acute pain, chronic pain, visceral pain, inflammatory pain, or neuropathic pain, as well as irritable bowel syndrome, Crohns disease, epilepsy, partial and generalized tonic seizures, multiple sclerosis, bipolar disease, and tachy-arrhythmias by the administration of an effective amount of aryl-link-aryl thiazolidine-dione and aryl-link-aryl oxazolodine-dione compounds, either alone, or in combination with one or more therapeutically active compounds, are described.